Human Phenotype Ontology 
Grandparent Node:
Clinical modifier (HP:0012823)help
Parent Node:
Pain characteristic (HP:0025280)help
..Starting node
Sharp (HP:0025281)help
Term ID: 25281
Name: Sharp
Definition: Applied to pain that is described as sharp, i.e., sudden and severe.
Reference: HP:0025281
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandDull (HP:0025282) help
..expandSleep-interrupting (HP:0025284) help
..expandTender (HP:0025283) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025281HP:0025281Sharp0 CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.